A Study of Residual Curarization Incidence in China

NCT01690338 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 6090

Last updated 2013-05-24

No results posted yet for this study

Summary

The purpose of this study is to determine the incidence of residual curarization in PACU and relevant risk factors.

Conditions

  • Perioperative/Postoperative Complications
  • PORC (Postoperative Residual Curarization)

Interventions

DRUG

Vecuronium Bromide

Administrative protocol of Vecuronium Bromide is determined by each caregiver's clinical experience.

DRUG

Rocuronium

Administrative protocol of rocuronium is determined by each caregiver's clinical experience.

DRUG

Cisatracurium

Administrative protocol of cisatracurium is determined by each caregiver's clinical experience

Sponsors & Collaborators

  • Ruijin Hospital

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Eastern Hepatobiliary Surgery Hospital

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Zhujiang Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • First Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • The First Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • Tianjin Medical University General Hospital

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Central South University

    collaborator OTHER
  • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • First Affiliated Hospital of Zhejiang University

    collaborator OTHER
  • China Medical University Hospital

    collaborator OTHER
  • Hebei Medical University Fourth Hospital

    collaborator OTHER
  • Tongji Hospital

    collaborator OTHER
  • Peking University First Hospital

    lead OTHER

Principal Investigators

  • Xinmin Wu, Doctor · Peking University First Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2014-10-31
Completion
2014-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01690338 on ClinicalTrials.gov